A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611711



Internal ID16399120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:87277222..87348886hg38UCSC Ensembl
Innerchr8:88289450..88361114hg19UCSC Ensembl
Innerchr8:88358566..88430230hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3871665
hg1971665
hg1871665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117706
Samples
Known GenesCNBD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611711
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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